PERFLUOROALKYLATED BENZOATE SURFACTANTS

Abstract

Provided are new compounds based on salts of aromatic acids containing perfluoroalkyl substituents. The compounds can be used as surfactants.

Description

FIELD OF INVENTION

The present invention is directed to compounds based on salts of aromatic acids containing perfluoroalkyl substituents. The compounds can be used as surfactants.

BACKGROUND

Aryl compounds bearing long fluoroalkyl chains have been used as ligands, as building blocks for advanced materials or biologically active compounds for pharmaceutical or agrochemical applications. They could also be useful for a wide variety of applications where surfactant properties are desired and/or needed. However few aryl compounds have been shown to be effective in these applications.

What is needed therefore are new aryl compounds with fluoroalkyl substituents which exhibit surfactant properties.

SUMMARY

One aspect of the present invention is a compound of Formula I, II or III:

wherein M is a univalent cation, R_f is independently a 1-8 carbon perfluoroalkyl group optionally substituted with ether oxygens, R′_f is a perfluoroalkylene containing at least two carbons, and R″_f is a perfluoroalkyl group containing at least two carbons.

Another aspect of the present invention is a surfactant comprising a compound having a Formula selected from 1, 11 and III wherein M is Na⁺, K⁺, NH₄⁺, Li⁺, Cs⁺, Rb⁺, or NR′R″R′″R″″⁺, where R′, R″, R′″, R″″ are independently a 1-6 carbon, linear or cyclic, alkyl or aromatic group.

A further aspect of the present invention is a method of forming an emulsion comprising: a) preparing a mixture comprising a fluorinated compound, water, and a compound having a formula selected from Formulae I to IV:

wherein M is Na⁺, K⁺, NH₄⁺, Li⁺, Cs⁺, Rb⁺, or NR′R″R′″R″″⁺, where R′, R″, R′″, R″″ are independently a 1-6 carbon, linear or cyclic, alkyl or aromatic group, R_f is independently a 1-8 carbon perfluoroalkyl group optionally substituted with ether oxygens, R′_f is a perfluoroalkylene containing at least two carbons, R″_f is a perfluoroalkyl group containing at least two carbons, and R²_f is independently a 1-8 carbon perfluoroalkyl group; and b) agitating the mixture until an emulsion is formed.

Another aspect of this invention is a method of altering the surface energy or interfacial free energy of a medium, said method comprising: a) providing a medium; and b) incorporating one or more compounds having a formula selected from Formulae I to IV.

DETAILED DESCRIPTION

In one embodiment, the present invention provides compounds of Formulae I, II, and III:

wherein M is a univalent cation, R_f is independently a 1-8 carbon perfluoroalkyl group optionally substituted with ether oxygens, R′_f is a perfluoroalkylene containing at least two carbons, and R″_f is a perfluoroalkyl group containing at least two carbons.

By “perfluorinated alkyl” is meant a univalent group containing carbon and fluorine connected by single bonds, and optionally substituted with ether oxygens. Common examples of such perfluorinated alkyl groups include perfluorinated methyl, ethyl, propyl, isopropyl, butyl, s-butyl, isobutyl, pentyl, neopentyl, hexyl, heptyl, isoheptyl, 2-ethylhexyl, cyclohexyl and octyl, optionally substituted with one or more ether oxygens. By “perfluorinated alkylene” is meant the divalent derivative of perfluorinated alkyl, as defined above. Typically R_f is independently a 4 to 6 carbon perfluoroalkyl, C₂F₅, C₃F₇, C₄F₉, C₅F₁₁, C₆F₁₃, CF₂CF₂OC₂F₅, CF₂CF₂OC₃F₇, or —(CF₂)_m—X_0-1—CF₂—X′_0-1—(CF₂)_nF wherein X and X′ are O, m is 1 to 6, and n is 1 to 6. Typically R_f″ is a 2 to 6 carbon perfluoroalkyl or C₂F₅, and R′_f is a 2 to 6 carbon perfluoroalkyl or C₂F₄.

M can be a single cation or a mixture of one or more univalent cations, such as H⁺, Na⁺, K⁺, NH₄⁺, Li⁺, Cs⁺, Rb⁺, or NR′R″R′″R″″⁺, where R′, R″, R′″, R″″ are independently a 1-6 carbon, linear or cyclic, alkyl or aromatic group. Typically M is H⁺, Na⁺, or K⁺.

Compounds of Formulae I to III can be prepared by any method known in the art. For Formulae I and II, one such method is the Heck coupling of aryl halides with commercially available fluoroalkyl-substituted ethylenes:

The resultant compositions can be reacted with a suitable base to produce the corresponding salts.

The Heck reaction is well known in the art and is described, for example, in Fine Chemical Synthesis—Homogeneous, Section 3.2. “The Heck Arylation Reaction”, J. G. de Vries, Encyclopedia of Catalysis, 2002 by John Wiley & Sons, Inc., http://dx.doi.org/10.1002/0471227617.eoc090

Any standard palladium Heck catalyst can be used, typically catalysts such as PdCl₂, Pd(OCOCH₃)₂ as such or in combination with (C₆H₅)₃P or (o-tolyl)₃P, or other P containing Pd complexes such as di(μ-acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium. The reaction is typically performed in a solvent, such as DMF or aqueous DMF, and in the presence of a base such as triethylamine, a mineral base such as potassium or sodium carbonate, KOCOCH₃, or K₂HPO₄. The reaction should be done under an inert atmosphere due to catalyst sensitivity. Reaction temperature is typically about 50° C. to 150° C. for about 24-72 hours. The di-substituted product can be achieved by adding the olefin and catalyst in quantities sufficient for exhaustive olefination of the C-halide bonds on the aromatic ring.

For compounds of Formula III, one method to prepare the compounds is via the reaction of iodo-substituted benzoic acids with at least stoichiometric amounts of copper:

This reaction is described in Neubert et al, Liquid Crystals, Vol 32, 2005, 781-795. The resultant compounds can be reacted with a base to produce the corresponding salts. The reaction is typically performed in a solvent, such as DMSO. Reaction temperature is typically run at about 90° C. to 150° C. for about 1-6 hours.

The products may be isolated by any suitable method known in the art, such as filtration, precipitation, and/or extraction. The compounds where M is H can be converted to the salt form either before or after isolation using methods well known in the art.

Compounds described herein wherein M is not H⁺ have been found effective in reducing the surface tension of liquids. Similarly, the compositions described herein can improve the wetting of a surface of a substrate by a liquid or coating mixture. Therefore, they are useful as surfactants in applications such as coating compositions, foams, fiber or surface protection, stabilizing dispersions, and emulsion reactions. The compositions are particularly useful in forming emulsions or dispersions with other fluorinated compounds and polymers.

By the term surfactant, or surface-active agent, is meant a substance that, when present at low concentration in a system, can adsorb onto surfaces or interfaces of the system and alter the surface or interfacial free energies of these surfaces. (Milton J. Rosen, “Surfactants and Interfacial Phenomena,” Second Ed., John Wiley & 10 Sons, New York, N.Y., 1989, page 1, DOI: 10.1002/0471670561). The term interface indicates a boundary between any two immiscible phases; the term surface denotes an interface where one phase is a gas, usually air.

According to other embodiments, there is provided a method of forming an emulsion comprising: a) preparing a mixture comprising a fluorinated compound, water, and one or more compounds having a formula selected from Formulae I to IV:

wherein M is Na⁺, K⁺, NH₄⁺, Li⁺, Cs⁺, Rb⁺, or NR′R″R′″R″″⁺, where R′, R″, R′″, R″″ are independently a 1-6 carbon, linear or cyclic, alkyl or aromatic group, R_f is independently a 1-8 carbon perfluoroalkyl group optionally substituted with ether oxygens, R′_f is a perfluoroalkylene containing at least two carbons, R′_f is a perfluoroalkyl group containing at least two carbons, and R²_f is independently a 1-8 carbon perfluoroalkyl group; and b) agitating the mixture until an emulsion is formed.

In other embodiments, there are provided methods for altering the surface energy of a medium, said method comprising a) providing a medium and b) incorporating one or more compounds having a formula selected from Formulae I to IV, wherein M, R_f, R′_f R″_f and R²_f are as described above, with the proviso that M is not H⁺. The medium can be any liquid composition or mixture but is typically water or an organic liquid or mixture.

EXAMPLES

Example 1

Synthesis of P-Perfluorohexylbenzoic Acid

A mixture of perfluorohexyl iodide (11.5 g), p-iodobenzoic acid (5.0 g), copper powder (4.5 g), and DMSO (40 mL) was stirred at 100° C. for 15 min and then at 110° C. for 1.5 h. The mixture was poured into 500 mL of water. Concentrated. HCl (20 mL) was added, and the mixture was stirred for 5 min. The solids were separated by filtration, washed with water, dried, and extracted with ether. The combined blue ether extracts were evaporated to dryness and the solid residue was dissolved in a solution of KOH (11 g) in water (200 mL). The solution was filtered to separate a small quantity of dark solids. After the filtrate was acidified with conc. HCl, the precipitated white p-perfluorohexylbenzoic acid was separated by filtration, thoroughly washed with water, and dried under vacuum. The yield was 6.54 g (74%). Anal. calcd for C₁₃H₅O₂F₁₃, %: C, 35.5; H, 1.1. Found, %: C, 35.0; H, 1.4. ¹H NMR (dmso-d₆), δ: 7.85 (d, J=8.3 Hz, 2H, arom. H), 8.2 (d, J=8.3 Hz, 2H, arom. H), 13.5 (br s, 1H COOH). ¹⁹F NMR (dmso-d₆), δ: −82.7 (t, J=9.8 Hz, 3F, CF₃), −112.4 (t, J=13.9 Hz, 2F, CF₂), −123.6 (m, 2F, CF₂), −123.9 (m, 2F, CF₂), −124.9 (m, 2F, CF₂), −128.1 (m, 2F, CF₂).

Example 2

Preparation of Potassium P-Perfluorohexylbenzoate

A mixture of p-perfluorohexylbenzoic acid (1.00 g), KHCO₃ (0.22 g), and water (20 mL) was stirred at heating and slowly brought almost to boil. After CO₂ evolution had ceased and a solid-free solution was formed the mixture was evaporated to dryness. The white residue was washed with acetone, then ether, and dried under vacuum. The yield of the potassium salt was 0.99 g (94%). Anal. Calcd for C₁₃H₄KO₂F₁₃, %: C, 32.6; H, 0.8. Found, %: C, 32.1; H, 0.9. ¹H NMR (D₂O), δ: 7.5 (d, J=8.3 Hz, 2H, arom. H), 7.9 (d, J=8.3 Hz, 2H, arom. H). ¹⁹F NMR (D₂O), δ: −82.6 (br s, 3F, CF₃), −111.6 (t, J=13.6 Hz, 2F, CF₂), −122.6 (br m, 2F, CF₂), −122.8 (br m, 2F, CF₂), −124.0 (br m, 2F, CF₂), −127.5 (br m, 2F, CF₂).

Example 3

Preparation of Sodium P-Perfluorohexylbenzoate

A mixture of p-perfluorohexylbenzoic acid (1.00 g), NaHCO₃ (0.185 g), and water (20 mL) was stirred at heating and slowly brought almost to boil. After CO₂ evolution had ceased and a solid-free solution was formed, the mixture was evaporated to dryness. The white residue was washed with acetone, then ether, and dried under vacuum. The yield of the sodium salt was 1.01 g (99%). Anal. Calcd for C₁₃H₄NaO₂F₁₃, %: C, 33.8; H, 0.9. Found, %: C, 33.5; H, 1.0. ¹H NMR (D₂O), δ: 7.7 (d, J=8.0 Hz, 2H, arom. H), 8.0 (d, J=8.0 Hz, 2H, arom. H). ¹⁹F NMR (D₂O), δ: −81.4 (br s, 3F, CF₃), −111.0 (br m, 2F, CF₂), −121.9 (br m, 2F, CF₂), −122.7 (br m, 2F, CF₂), −123.3 (br m, 2F, CF₂), −126.6 (br m, 2F, CF₂). The compounds prepared in Examples 2 and 3 were evaluated for surfactancy using a Kruss K11 Tensiometer at 22.1° C. Mixtures of the compounds and distilled water were prepared using a sonicator at a series of dilutions, up to 1% (weight of water/weight of compound). As can be seen in Table 1 below, the surface tension of the mixture decreased as the concentration increased.

	TABLE 1
			Surface	Std.
		Concentration	Tension	Dev.
	Sample	w/w %	mN/m	mN/m
	DI Water	0	73.3	0.1
	Ex. 2	0.0001	67.8	0.1
		0.001	48.8	0.1
		0.01	42.6	0.1
		0.1	27.1	0.1
		1	19.2	0.1
	DI Water	0	73.3	0.1
	Ex. 3	0.0001	56.5	0.1
		0.001	51.1	0.1
		0.01	45.2	0.1
		0.1	31.2	0.1
		1	18.7	0.1

Example 4

Synthesis of P-Perfluorobutylbenzoic Acid

A mixture of perfluorobutyl iodide (10.6 g), p-iodobenzoic acid (5.75 g), copper powder (5.2 g), and DMSO (40 mL) was stirred in a sealed thick-wall reactor first at 70° C. for 20 min, then at 100° C. for 30 min, and finally at 110° C. for 1 h 40 min. The mixture was poured into 500 mL of water. Conc. HCl (30 mL) was added, and the mixture was stirred for 30 min. The solids were separated by filtration, washed with water, dried, and extracted with ether. The combined ether extracts were evaporated to dryness and the solid residue was stirred with a solution of KOH (15 g) in water (200 mL) for 30 min. The resulting solution was filtered to separate a small quantity of blue solids. After the filtrate was acidified with conc. HCl, the precipitated white p-perfluorobutylbenzoic acid was separated by filtration, thoroughly washed with water, and dried under vacuum. The yield was 4.4 g (56%). Anal. Calcd for C₁₁H₅O₂F₉, %: C, 38.8; H, 1.5. Found, %: C, 38.3; H, 1.5. ¹H NMR (dmso-d₆), δ: 7.85 (d, J=8.3 Hz, 2H, arom. H), 8.2 (d, J=8.3 Hz, 2H, arom. H), 13.5 (br s, 1H COOH). ¹⁹F NMR (dmso-d₆), δ: −80.9 (tm, J=9.7 Hz, 3F, CF₃), −110.6 (tm, J=12.7 Hz, 2F, CF₂), −122.8 (m, 2F, CF₂), −125.6 (m, 2F, CF₂).

Example 5

Preparation of Sodium P-Perfluorobutylbenzoate

A mixture of p-perfluorobutylbenzoic acid (1.00 g), NaHCO₃ (0.24 g), and water (20 mL) was stirred at heating and slowly brought almost to boil. After CO₂ evolution had ceased and a solid-free solution was formed the mixture was evaporated to dryness. The white residue was washed with acetone, then ether, and dried under vacuum. The yield of the sodium salt was 0.97 g (94%). Anal. Calcd for C₁₁H₄NaO₂F₉, %: C, 36.5; H, 1.1. Found, %: C, 36.0; H, 1.1. ¹H NMR (D₂O), δ: 7.75 (d, J=8.4 Hz, 2H, arom. H), 8.0 (d, J=8.4 Hz, 2H, arom. H). ¹⁹F NMR (D₂O), δ: −81.4 (tt, J=9.9 Hz and 3.3 Hz, 3F, CF₃), −111.1 (dm, J=13.0 Hz, 2F, CF₂), −123.4 (m, 2F, CF₂), −125.9 (m, 2F, CF₂).

Example 6

Synthesis of P-Trans-Perfluorobutylvinylidenebenzoic Acid

A mixture of p-bromobenzoic acid (8.0 g), Na₂CO₃ (10.0 g), and water (40 mL) was brought to boil at stirring and then cooled to room temperature. Perfluorobutylethylene (15 mL) in DMF (80 mL) and trans-di(μ-acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium (0.38 g; prepared as described in: Herrmann et al., Chem. Eur. J. 1997, 3, 1357) were added, and the mixture was stirred sealed under N₂ in a thick wall reactor at 100 C.° for 72 h. After cooling to room temperature the reactor was unsealed and the contents were poured into 800 mL of water. At stirring, conc. HCl (20 mL) was added, after which the precipitate was separated by filtration, washed with water, and dried under vacuum. The crude product was purified using toluene solvent and a Soxhlet extractor fitted with two nested thimbles, in which the inner thimble contained the material to be purified, and the space between the inner and outer thimble contained silica gel, as described by Halliday, Young and Grushin, Org. Lett. 2003, 5, 2003. After the extraction was complete, the toluene solution was reduced in volume and cooled in an ice bath for 2-3 h. The white crystalline solid was separated by filtration, washed with a small quantity of cold toluene, and dried under vacuum. The yield of p-trans-perfluorobutylvinylidenebenzoic acid was 7.38 g (51%). ¹H NMR (dmso-d₆), δ: 6.9 (dt, J=16.2 and 12.8 Hz, 1H, CHCF₂), 7.45 (dt, J=16.2 and 1.9 Hz, 1H, CH—C₆H₄), 7.9 (d, J=8.4 Hz, 2H, arom. H), 8.0 (d, J=8.4 Hz, 2H, arom. H), 13.1 (br s, 1H COOH). ¹⁹F NMR (dmso-d₆), δ: −80.9 (tm, J=9.5 Hz, 3F, CF₃), −110.6 (m, 2F, CF₂), −123.9 (m, 2F, CF₂), −125.7 (m, 2F, CF₂).

Example 7

Preparation of Sodium P-Trans-Perfluorobutylvinylidenebenzoate

A mixture of p-trans-perfluorobutylvinylidenebenzoic acid (7.38 g), NaHCO₃ (1.62 g), and water (50 mL) was stirred at heating and slowly brought almost to boil. After CO₂ evolution had ceased and a solid-free solution was formed the mixture was evaporated to dryness. The white residue was washed with ether and dried under vacuum. The yield of the sodium salt was 7.41 g (99%). Anal. Calcd for C₁₃H₆NaO₂F₉, %: C, 40.2; H, 1.6. Found, %: C, 40.4; H, 1.9. ¹H NMR (D₂O), δ: 6.3 (dt, J=16.0 and 12.3 Hz, 1H, CHCF₂), 7.1 (dt, J=16.0 and 2.0 Hz, 1H, CH—C₆H₄), 7.4 (d, J=8.3 Hz, 2H, arom. H), 7.8 (d, J=8.3 Hz, 2H, arom. H). ¹⁹F NMR (D₂O), δ: −82.1 (tm, J=9.6 Hz, 3F, CF₃), −112.0 (m, 2F, CF₂), −125.0 (m, 2F, CF₂), −126.5 (m, 2F, CF₂).

Example 8

Synthesis of P-3-Oxaperfluoropentylbenzoic Acid

A mixture of 3-oxaperfluoropentyl iodide (11.0 g), p-iodobenzoic acid (5.0 g), copper powder (4.5 g), and DMSO (40 mL) was vigorously stirred as the temperature was slowly raised from 25° C. to 100° C. within 1 h, and then to 110° C. Agitation was continued for 1.5 h at 110° C., after which the mixture was allowed to cool below 100° C. and poured into 500 mL of water. Concentrated. HCl (30 mL) was added, and the mixture was stirred for 5 min. The solids were separated by filtration, washed with water, dried, and extracted with ether. The combined ether extracts were evaporated to dryness and the solid residue was dissolved in a solution of KOH (10 g) in water (200 mL). The solution was filtered to separate minor insolubles a small quantity of dark solids, and the filtrate was acidified with conc. HCl. The precipitated white p-3-oxaperfluoropentylbenzoic acid was separated by filtration, thoroughly washed with water, and dried under vacuum. The yield was 1.81 g (25%). Anal. calcd for C₁₁H₅O₃F₉, %: C, 37.1; H, 1.4. Found, %: C, 36.9; H, 1.5. ¹H NMR (dmso-d₆), δ: 7.8 (d, J=8.3 Hz, 2H, arom. H), 8.2 (d, J=8.3 Hz, 2H, arom. H), 13.5 (br s, 1H COOH). ¹⁹F NMR (dmso-d₆), δ: −86.6 (br s, 3F, CF₃), −87.1 (m, 2F, CF₂), −88.6 (m, 2F, CF₂), −114.4 (br s, 2F, CF₂).

Example 9

Preparation of sodium P-3-Oxaperfluoropentylbenzoate

A mixture of p-3-oxaperfluoropentylbenzoic acid (1.20 g), NaHCO₃ (0.28 g), and water (50 mL) was stirred at heating and slowly brought to boil. After CO₂ evolution had ceased and a solid-free solution was formed the mixture was evaporated to dryness. The residue was washed with acetone, then ether, and dried under vacuum. The yield of the sodium salt was 1.4 g (90%). Anal. calcd for C₁₁H₄O₃F₉Na, %: C, 34.9; H, 1.1. Found, %: C, 34.7; H, 1.2. ¹H NMR (D₂O), δ: 7.8 (d, J=8.3 Hz, 2H, arom. H), 8.0 (d, J=8.3 Hz, 2H, arom. H) ¹⁹F NMR (D₂O), δ: −87.1 (br s, 3F, CF₃), −87.7 (m, 2F, CF₂), −88.9 (m, 2F, CF₂), −115.1 (br t, 2F, CF₂).

Claims

1. A compound of Formula I, II, or III:

wherein M is a univalent cation, Rf is independently a 1-8 carbon perfluoroalkyl group optionally substituted with ether oxygens, R′f is a perfluoroalkylene containing at least two carbons, and R″f is a perfluoroalkyl group containing at least two carbons.

2. The compound of claim 1 wherein Rf is —(CF2)m—X0-1—CF2—X′0-1—(CF2)nF wherein X and X′ are O, m is 1 to 6, and n is 1 to 6.

3. The compound of claim 1 wherein Rf″ is C2F5 and R′f is C2F4.

4. The compound of claim 1 wherein Rf is C4F9, C6F13, CF2CF2OC2F5, or CF2CF2OC3F7.

5. The compound of claim 1 wherein M is H+, Na+, K+, NH4+, Li+, Cs+, Rb+, or NR′R″R′″R″″+, where R′, R″, R′″, R″″ are independently a linear or cyclic 1-6 carbon, alkyl or aromatic group.

6. A surfactant comprising the compound of claim 1 wherein M is Na+, K+, NH4+, Li+, Cs+, Rb+, or NR′R″R′″R″″+, where R′, R″, R′″, R″″ are independently a 1-6 carbon, linear or cyclic, alkyl or aromatic group.

7. A method of forming an emulsion comprising: wherein M is Na+, K+, NH4+, Li+, Cs+, Rb+, or NR′R″R′″R″″+, where R′, R″, R′″, R″″ are independently a 1-6 carbon, linear or cyclic, alkyl or aromatic group, Rf is independently a 1-8 carbon perfluoroalkyl group optionally substituted with ether oxygens, R′f is a perfluoroalkylene containing at least two carbons, R″f is a perfluoroalkyl group containing at least two carbons, and R2f is independently a 1-8 carbon perfluoroalkyl group; and

a) preparing a mixture comprising a fluorinated compound, water, and one or more compounds having a formula selected from Formulae I to IV:

b) agitating the mixture until an emulsion is formed.

8. The method of claim 7 wherein Rf is (CF2)m—X0-1—CF2X0-1—(CF2)nF wherein X and X′ are O, m is 1 to 6, and n is 1 to 6.

9. The method of claim 7 wherein Rf″ is C2F5 and R′f is C2F4.

10. The method of claim 7 wherein Rf is C4F9, C6F13, CF2CF2OC2F5, or CF2CF2OC3F7.

11. A method of altering the surface energy of a medium, said method comprising: wherein M is Na+, K+, NH4+, Li+, Cs+, Rb+, or NR′R″R′″R″″+, where R′, R″, R′″, R″″ are independently a 1-6 carbon, linear or cyclic, alkyl or aromatic group, Rf is independently a 1-8 carbon perfluoroalkyl group optionally substituted with ether oxygens, R′f is a perfluoroalkylene containing at least two carbons, R″f is a perfluoroalkyl group containing at least two carbons, and R2f is independently a 1-8 carbon perfluoroalkyl group.

a) providing a medium and

b) incorporating into the medium one or more compounds having a formula selected from Formulae I to IV: